{
    "disease_id": "DOID:0080225",
    "recommended_name": {
        "id": "DOID:0080225",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080225",
        "name": "amyotrophic lateral sclerosis type 23",
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in heterozygous mutation in the ANXA11 gene on chromosome 10q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0027694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027694",
            "name": "amyotrophic lateral sclerosis type 23",
            "description": ""
        },
        {
            "id": "MONDO:0027694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027694",
            "name": "ALS23",
            "description": ""
        },
        {
            "id": "MONDO:0027694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0027694",
            "name": "amyotrophic lateral sclerosis 23",
            "description": ""
        },
        {
            "id": "MIM:617839",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617839",
            "name": "Amyotrophic lateral sclerosis 23",
            "description": "Amyotrophic lateral sclerosis 23"
        }
    ]
}